NR1H4_HUMAN - dbPTM
NR1H4_HUMAN - PTM Information in dbPTM
Basic Information of Protein
UniProt ID NR1H4_HUMAN
UniProt AC Q96RI1
Protein Name Bile acid receptor
Gene Name NR1H4
Organism Homo sapiens (Human).
Sequence Length 486
Subcellular Localization Nucleus .
Isoform 1: Nucleus .
Isoform 2: Nucleus .
Isoform 3: Nucleus .
Isoform 4: Nucleus .
Protein Description Ligand-activated transcription factor. Receptor for bile acids (BAs) such as chenodeoxycholic acid (CDCA), lithocholic acid, deoxycholic acid (DCA) and allocholic acid (ACA). Plays a essential role in BA homeostasis through the regulation of genes involved in BA synthesis, conjugation and enterohepatic circulation. Also regulates lipid and glucose homeostasis and is involved innate immune response. [PubMed: 10334992]
Protein Sequence MVMQFQGLENPIQISPHCSCTPSGFFMEMMSMKPAKGVLTEQVAGPLGQNLEVEPYSQYSNVQFPQVQPQISSSSYYSNLGFYPQQPEEWYSPGIYELRRMPAETLYQGETEVAEMPVTKKPRMGASAGRIKGDELCVVCGDRASGYHYNALTCEGCKGFFRRSITKNAVYKCKNGGNCVMDMYMRRKCQECRLRKCKEMGMLAECMYTGLLTEIQCKSKRLRKNVKQHADQTVNEDSEGRDLRQVTSTTKSCREKTELTPDQQTLLHFIMDSYNKQRMPQEITNKILKEEFSAEENFLILTEMATNHVQVLVEFTKKLPGFQTLDHEDQIALLKGSAVEAMFLRSAEIFNKKLPSGHSDLLEERIRNSGISDEYITPMFSFYKSIGELKMTQEEYALLTAIVILSPDRQYIKDREAVEKLQEPLLDVLQKLCKIHQPENPQHFACLLGRLTELRTFNHHHAEMLMSWRVNDHKFTPLLCEIWDVQ
Overview of Protein Modification Sites with Functional and Structural Information
Experimental Post-Translational Modification Sites

* ASA = Accessible Surface Area

Locations Modification Substrate Peptides
&
Secondary Structure
ASA (%) Reference Orthologous
Protein Cluster
31PhosphorylationGFFMEMMSMKPAKGV
CHHHHHHCCCCCCCC
23.5024719451
62 (in isoform 1)O-linked_Glycosylation-5.2224037988
132SumoylationGASAGRIKGDELCVV
CCCCCCCCCCEEEEE
59.9723546875
135PhosphorylationAGRIKGDELCVVCGD
CCCCCCCEEEEEECC
53.3818755856
145PhosphorylationVVCGDRASGYHYNAL
EEECCCCCCCCCEEE
40.5518755856
154PhosphorylationYHYNALTCEGCKGFF
CCCEEEECCCCCHHH
4.3818755856
164PhosphorylationCKGFFRRSITKNAVY
CCHHHHCCCCCCCEE
30.2818755856
167AcetylationFFRRSITKNAVYKCK
HHHCCCCCCCEEECC
41.0422345554
210MethylationLAECMYTGLLTEIQC
HHHHHHHHHHHHHHH
10.9522345554
220MethylationTEIQCKSKRLRKNVK
HHHHHCHHHHHHHHH
40.7322345554
227AcetylationKRLRKNVKQHADQTV
HHHHHHHHHHHHHCC
45.8418668687
289SumoylationEITNKILKEEFSAEE
HHHHHHHHHHCCHHH
59.6823546875
356PhosphorylationIFNKKLPSGHSDLLE
HHHCCCCCCCHHHHH
60.6223403867
359PhosphorylationKKLPSGHSDLLEERI
CCCCCCCHHHHHHHH
33.2223403867
369PhosphorylationLEERIRNSGISDEYI
HHHHHHHCCCCCHHH
27.88-
372PhosphorylationRIRNSGISDEYITPM
HHHHCCCCCHHHHHH
28.10-
456PhosphorylationGRLTELRTFNHHHAE
HHHHHCCCCCHHHHH
41.2223462506
467PhosphorylationHHAEMLMSWRVNDHK
HHHHHHHHEEECCCC
14.04-

Upstream regulatory proteins (kinases for phosphorylation sites, E3 ubiquitin ligases of ubiquitination sites, ...)
Modified Location Modified Residue Modification Type of Upstream Proteins Gene Name of Upstream Proteins UniProt AC of Upstream Proteins Sources
77YPhosphorylationKinaseSRCP12931
PSP
145SPhosphorylationKinasePRKCAP17252
Uniprot
164SPhosphorylationKinasePRKCAP17252
Uniprot
456TPhosphorylationKinasePRKCZQ05513
Uniprot

Functions of PTM Sites
Modified Location Modified Residue Modification Function Reference
227KAcetylation

19883617

Disease-associated PTM Sites based on SAP

* Distance = the distance between SAP position and PTM sites.

Modified Location Modification Variant Position
(Distance <= 10)
Residue Change SAP Related Disease Reference

Oops, there are no SNP-PTM records of NR1H4_HUMAN !!

Protein-Protein Interaction
Interacting Protein Gene Name Interaction Type PPI Reference Domain-Domain Interactions
NCOA1_HUMANNCOA1physical
11136553
RXRA_HUMANRXRAphysical
7760852
PRKDC_HUMANPRKDCphysical
19833092
XRCC6_HUMANXRCC6physical
19833092
XRCC5_HUMANXRCC5physical
19833092
ANM1_HUMANPRMT1physical
15911693
H31_HUMANHIST1H3Aphysical
15471871
RXRA_HUMANRXRAphysical
19883617
G3P_HUMANGAPDHphysical
15604093
RXRG_HUMANRXRGphysical
15604093
ESR1_HUMANESR1physical
17333335
NCOR2_HUMANNCOR2physical
16219912
SUMO1_HUMANSUMO1physical
23546875
RXRB_HUMANRXRBphysical
28514442

Drug and Disease Associations
Kegg Disease
There are no disease associations of PTM sites.
OMIM Disease
There are no disease associations of PTM sites.
Kegg Drug
There are no disease associations of PTM sites.
DrugBank
DB06777Chenodeoxycholic acid
Regulatory Network of NR1H4_HUMAN

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Related Literatures of Post-Translational Modification

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